1. Identification of the Major Intestinal Fatty Acid Transport Protein
Andreas Stahl, David J Hirsch, Ruth E Gimeno, Sandhya Punreddy, Pei Ge, Nicki Watson, Shraddha Patel, Mariana Kotler, Alejandra Raimondi, Louis A Tartaglia, Harvey F Lodish 
Molecular Cell 
Volume 4, Issue 3, Pages (September 1999)
DOI: /S (00)

2. Figure 1 FATP4 Mediates LCFA Uptake
(A) Mammalian expression constructs containing either hsFATP4 (squares and triangles) or empty control vector (circles) were stably transfected into 293 cells. Short-term uptake of Bodipy-FA in the presence of BSA was determined by FACS. The mean fluorescence of the viable cell population is expressed in arbitrary fluorescence units. FATP4 protein expression was determined by densitometry of anti-FATP4 Western blots, shown in the insert, and is expressed in arbitrary units.
(B) Short-term uptake of Bodipy-palmitate (1 μM), either by control cells (black bars) or FATP4-expressing cells (hatched bars), was measured in the presence of 0, 10, or 100 μM unlabeled palmitate. FA uptake was quantified by FACS and expressed in arbitrary fluorescence units.
(C) The rate of [3H]palmitate uptake by 293 cells, which were stably transfected with a construct for either human FATP4 (diamonds) or an empty vector (circles), was compared to that of isolated enterocytes (squares).
Molecular Cell 1999 4, DOI: ( /S (00) )

3. Figure 2 FATP4 Is Localized in Enterocytes by In Situ Hybridization
(A) In situ hybridization of a section through a whole E18.5 embryo (left panel) and sections through the small intestine of E18.5 embryo (right panels) with a FATP4-specific riboprobe shown at 200× in phase contrast and dark field.
(B) In situ hybridization of a section through duodenum, ileum, and colon of adult mice with FATP4- and FATP5-specific riboprobes shown at 200× in dark field and phase contrast.
Molecular Cell 1999 4, DOI: ( /S (00) )

4. Figure 3
FATP4 Is the Prevalent Member of the FATP Family in the Ileum and Jejunum
Northern blot analysis of the expression patterns of hsFATP1 through hsFATP6 in the ileum and jejunum. Probes were from unique region of the genes and did not cross-react with other FATP members. As a control, all probes were hybridized under similar conditions to mRNAs from a variety of FATP-expressing tissues. FATP1, heart; FATP2, kidney; FATP3, lung; FATP5, liver; FATP6, heart.
Molecular Cell 1999 4, DOI: ( /S (00) )

5. Figure 4
The FATP4 Protein Is Specifically Detected by a Polyclonal Antiserum
(A) Western blot of GST fusion proteins of the C termini of FATP2 through FATP5 with a polyclonal antiserum against the C terminus of FATP4.
(B) Western blot detection of FATP4 in enterocyte lysates from three different mice without or with preincubation of the antiserum with the antigen. Molecular mass standards are indicated in kDa.
Molecular Cell 1999 4, DOI: ( /S (00) )

6. Figure 5 FATP4 Is Located on the Apical Face of Enterocytes
Fluorescent and phase contrast pictures of murine small intestine. Fresh frozen thin sections were either incubated with preimmune (A) or anti-FATP4 serum (B). Confocal laser microscopy images of FATP4 in the small intestine at 20× (C) and 63× (D). Deconvolution microscopy of a small intestinal thin section (E) stained with anti-FATP4 (green) and DAPI (blue) at a 40× magnification.
Molecular Cell 1999 4, DOI: ( /S (00) )

7. Figure 6 FATP4 Is Present in the Microvilli
Immunoelectron microscopy of fresh frozen murine intestinal cells. Fresh frozen unfixed microsections of murine ileum were incubated with FATP4-specific antiserum, which was detected by 10 nm gold conjugated secondary antibodies. Longitudinal section through brush border membrane ([A], bar = 0.21 μM). Cross section through microvilli ([B], bar = 0.3 μM); arrows indicate the position of the gold particles. High magnification cross section through microvilli ([C], bar = 0.12 μM).
Molecular Cell 1999 4, DOI: ( /S (00) )

8. Figure 7 FATP4 Is Required for Efficient LCFA Uptake by Enterocytes
(A) The kinetics of [3H]oleate incorporation by enterocytes isolated from the small intestine of mice were measured after incubation for 48 hr in tissue culture either without oligonucleotides (squares) or with 100 μM FATP4-specific sense (circles) or antisense (diamonds) oligonucleotides.
(B) Isolated enterocytes were incubated for 48 hr with increasing concentrations of the FATP4 antisense oligonucleotide or with 100 μM of a randomized control oligonucleotide with identical nucleotide composition to the FATP4 antisense oligonucleotide. The uptake of oleate by the enterocytes was then measured over a 5 min time interval (solid bars). In parallel, the levels of FATP4 protein and, as a loading control, β-catenin, were determined by Western blotting and quantitated using densitometry (hatched bars). FA uptake and FATP4 protein levels were normalized to that of untreated cells. The averages and standard deviations of four independent experiments are shown.
(C) Uptake rates of [3H]oleate, [3H]palmitate, and [35S]methionine by primary enterocytes were measured after 48 hr incubation with either of two FATP4 antisense (solid bars) or randomized control oligonucleotide (hatched bars) at a concentration of 100 μM and expressed as percent of untreated cells.
Molecular Cell 1999 4, DOI: ( /S (00) )